ID: 84464 | SLX4 structure-specific endonuclease subunit [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (3581181..3611606, complement) | BTBD12, FANCP, MUS312 | 613278 |
ID: 83990 | BRCA1 interacting helicase 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (61679139..61863528, complement) | BACH1, FANCJ, OF | 605882 |
ID: 80233 | FA core complex associated protein 100 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81539891..81553133, complement) | C17orf70 | 611301 |
ID: 79728 | partner and localizer of BRCA2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (23603165..23641310, complement) | BROVCA5, FANCN, PNCA3 | 610355 |
ID: 57697 | FA complementation group M [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (45135930..45200890) | FAAP250, KIAA1596, POF15, SPGF28 | 609644 |
ID: 55215 | FA complementation group I [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (89243979..89317259) | KIAA1794 | 611360 |
ID: 55159 | ring finger and WD repeat domain 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (74621399..74666877, complement) | FANCW, RNF201 | 614151 |
ID: 55120 | FA complementation group L [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (58159243..58241380, complement) | FAAP43, PHF9, POG | 608111 |
ID: 29089 | ubiquitin conjugating enzyme E2 T [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (202331657..202341936, complement) | FANCT, HSPC150, PIG50 | 610538 |
ID: 10459 | mitotic arrest deficient 2 like 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (11674480..11691830, complement) | FANCV, MAD2B, POLZ2, REV7 | 604094 |
ID: 7516 | X-ray repair cross complementing 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (152644776..152676141, complement) | FANCU, POF17, SPGF50 | 600375 |
ID: 5889 | RAD51 paralog C [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (58692573..58735611) | BROVCA3, FANCO, R51H3, RAD51L2 | 602774 |
ID: 5888 | RAD51 recombinase [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (40694733..40732340) | BRCC5, FANCR, HRAD51, HsRad51, HsT16930, MRMV2A, RECA, RAD51 | 179617 |
ID: 2189 | FA complementation group G [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35073839..35079942, complement) | FAG, XRCC9 | 602956 |
ID: 2188 | FA complementation group F [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22622533..22625823, complement) | FAF | 613897 |
ID: 2187 | FA complementation group B [Homo sapiens (human)] | Chromosome X, NC_000023.11 (14689524..14873069, complement) | FA2, FAAP90, FAAP95, FAB, FACB | 300515 |
ID: 2178 | FA complementation group E [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (35452338..35467102) | FACE, FAE | 613976 |
ID: 2177 | FA complementation group D2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (10026437..10101932) | FA-D2, FA4, FACD, FAD, FAD2, FANCD | 613984 |
ID: 2176 | FA complementation group C [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95099054..95317709, complement) | FA3, FAC, FACC | 613899 |
ID: 2175 | FA complementation group A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89737549..89816647, complement) | FA, FA-H, FA1, FAA, FACA, FAH, FANCH | 607139 |